(Q36837415)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

title

Angucyclines and Angucyclinones from Streptomyces sp. CB01913 Featuring C-Ring Cleavage and Expansion (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

1 reference

Streptomyces tsusimaensis

1 reference

Streptomyces albidoflavus

1 reference

(3S,4R)-3,4-dihydroxy-8-methoxy-3-methyl-2,4-dihydrobenzo[a]anthracene-1,7,12-trione

1 reference

(3R)-3-hydroxy-7-(3-hydroxy-7-methoxy-1,3-dihydro-2-benzofuran-1-yl)-3-methyl-2,4-dihydronaphthalen-1-one

1 reference

3,6a,7,12-Tetrahydroxy-8-methoxy-3-methyl-3,4,6a,7,12,12a-hexahydrobenzo[a]anthracene-1(2H)-one

1 reference

6,12-dihydroxy-8-methoxy-3-methyl-1-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-12H-benzo[a]anthracen-7-one

1 reference

(3R)-7-[(1S,3S)-3-ethoxy-7-methoxy-2,3-dihydro-1H-inden-1-yl]-3-hydroxy-3-methyl-2,4-dihydronaphthalen-1-one

1 reference

(-)-8-O-Methyltetrangomycin

1 reference

(3R)-3,7-dihydroxy-8-[2-(hydroxymethyl)-3-methoxybenzoyl]-3-methyl-2,4-dihydronaphthalen-1-one

1 reference

(3R,8R,13R)-3alpha-Hydroxy-3-methyl-9-methoxy-8,13-epoxy-3,4,8,13-tetrahydrobenzo[e]naphtho[2,1-b]oxepin-1(2H)-one

1 reference

(3S)-12-hydroxy-8-methoxy-3-methyl-1-[(2R,3R,4R,5R,6R)-3,5,6-trihydroxy-4-methyloxan-2-yl]oxy-2,3,4,12-tetrahydro-1H-benzo[a]anthracen-7-one

1 reference

12-deoxo-12-hydroxy-8-O-methyltetrangomycin

1 reference

8-O-methyltetrangomycin

1 reference

(3R)-3-hydroxy-8-methoxy-3-methyl-6-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,4-dihydrobenzo[a]anthracene-1,7,12-trione

1 reference

1 reference

(3R)-3,12-dihydroxy-8-methoxy-3,12-dimethyl-6-[(3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,4-dihydrobenzo[a]anthracene-1,7-dione

1 reference

(3R)-3-hydroxy-7-[(1S,3S)-3-hydroxy-7-methoxy-2,3-dihydro-1H-inden-1-yl]-3-methyl-2,4-dihydronaphthalen-1-one

1 reference

(3R)-3-hydroxy-7-[(1S,3R)-3-hydroxy-7-methoxy-2,3-dihydro-1H-inden-1-yl]-3-methyl-2,4-dihydronaphthalen-1-one

1 reference

(3R,8S,13S)-3alpha-Hydroxy-3-methyl-9-methoxy-8,13-epoxy-3,4,8,13-tetrahydrobenzo[e]naphtho[2,1-b]oxepin-1(2H)-one

1 reference

1,4-dimethoxy-3-(3'-hydroxy-3'-methyl-1'-tetralon e)-1(3H)-isobenzofuran

1 reference

(3R)-7-[(1S,3R)-3-ethoxy-7-methoxy-2,3-dihydro-1H-inden-1-yl]-3-hydroxy-3-methyl-2,4-dihydronaphthalen-1-one

1 reference

(3R)-7-[(1S,3R)-3,7-dimethoxy-1,3-dihydro-2-benzofuran-1-yl]-3-hydroxy-3-methyl-2,4-dihydronaphthalen-1-one

1 reference

(3R,6aS,7S,12S,12aR)-3,6a,7,12-tetrahydroxy-8-methoxy-3-methyl-4,7,12,12a-tetrahydro-2H-benzo[a]anthracen-1-one

1 reference

(3S,6aR,7R,12R,12aS)-3,6a,7,12-tetrahydroxy-8-methoxy-3-methyl-4,7,12,12a-tetrahydro-2H-benzo[a]anthracen-1-one

1 reference

(3S,4R)-3,4,12-trihydroxy-8-methoxy-3,12-dimethyl-1-methylidene-2,4-dihydrobenzo[a]anthracen-7-one

1 reference

(3R)-3,8,12-trihydroxy-3-methyl-4,12-dihydro-2H-benzo[a]anthracene-1,7-dione

1 reference

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Jeffrey D. Rudolf

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Xiangcheng Zhu

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Christoph Rader

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

author name string

Ming Ma

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Mostafa E Rateb

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Qihui Teng

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Yong Huang

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Li-Xing Zhao

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Yi Jiang

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Xiuling Li

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Yanwen Duan

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Ben Shen

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

publication date

3 September 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

23 February 2020

https://europepmc.org/articles/pmc4845661?pdf=render

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1021/acs.jnatprod.5b00601?email=unpaywall_01@example.com

published in

Journal of Natural Products

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

volume

78

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

page(s)

2471-2480

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

issue

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1021/acs.jnatprod.5b00601?email=unpaywall_01@example.com

access restriction status

open access

1 reference

inferred from online access status

cites work

Strain prioritization for natural product discovery by a high-throughput real-time PCR method.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Description of Streptomonospora sediminis sp. nov. and Streptomonospora nanhaiensis sp. nov., and reclassification of Nocardiopsis arabia Hozzein & Goodfellow 2008 as Streptomonospora arabica comb. nov. and emended description of the genus Streptomo

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Medium optimization of Streptomyces sp. 17944 for tirandamycin B production and isolation and structural elucidation of tirandamycins H, I and J.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Isolation and structural elucidation of glucoside congeners of platencin from Streptomyces platensis SB12600.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Angucyclines from an insect-derived actinobacterium Amycolatopsis sp. HCa1 and their cytotoxic activity

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Antibiotic and antimalarial quinones from fungus-growing ant-associated Pseudonocardia sp.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Cytotoxic angucycline class glycosides from the deep sea actinomycete Streptomyces lusitanus SCSIO LR32.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Search method for inhibitors of Staphyloxanthin production by methicillin-resistant Staphylococcus aureus

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Angucyclines: Biosynthesis, mode-of-action, new natural products, and synthesis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Diverse metabolic profiles of a Streptomyces strain isolated from a hyper-arid environment

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Actinopolysporins A-C and tubercidin as a Pdcd4 stabilizer from the halophilic actinomycete Actinopolyspora erythraea YIM 90600

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Tirandamycins from Streptomyces sp. 17944 inhibiting the parasite Brugia malayi asparagine tRNA synthetase

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

11-Deoxylandomycinone and landomycins X-Z, new cytotoxic angucyclin(on)es from a Streptomyces cyanogenus K62 mutant strain

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Isolation, structure elucidation and biological activity of angucycline antibiotics from an epiphytic yew streptomycete

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Antimicrobial activities of jadomycin B and structurally related analogues

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Rearranged and unrearranged angucyclinones from Indonesian Streptomyces spp.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Agar and broth dilution methods to determine the minimal inhibitory concentration (MIC) of antimicrobial substances

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Angucyclinones from an Indonesian Streptomyces sp.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Antitumor agents from Streptomyces anandii: gilvocarcins V, M and E.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Tentative interpretive standards for agar disk diffusion antimicrobial susceptibility testing of cefoperazone

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Saquayamycins, new aquayamycin-group antibiotics

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Landomycins, new angucycline antibiotics from Streptomyces sp. I. Structural studies on landomycins A-D.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Angucycline group antibiotics

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Langkocyclines: novel angucycline antibiotics from Streptomyces sp. Acta 3034(*).

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Functional analysis of hatomarubigin biosynthesis genes and production of a new hatomarubigin using a heterologous expression system

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Waldiomycin, a novel WalK-histidine kinase inhibitor from Streptomyces sp. MK844-mF10.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Cytotoxic angucyclines from Amycolatopsis sp. HCa1, a rare actinobacteria derived from Oxya chinensis

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Angucyclinone antibiotics: total syntheses of YM-181741, (+)-ochromycinone, (+)-rubiginone B2, (-)-tetrangomycin, and MM-47755.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

The dynamic structure of jadomycin B and the amino acid incorporation step of its biosynthesis

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4845661

Studies on marine microorganisms. IV. A new antibiotic SS-228 Y produced by Chainia isolated from shallow sea mud

5 September 2018

1 reference

12 December 2020

Total synthesis of (-)-8-O-methyltetrangomycin (MM 47755)

1 reference

12 December 2020

New antitumor substances, BE-12406A and BE-12406B, produced by a streptomycete. II. Structure determination

1 reference

12 December 2020

Isolation and characterization of LS1924A, a new analog of emycins

1 reference

12 December 2020

Biosynthetic potential-based strain prioritization for natural product discovery: a showcase for diterpenoid-producing actinomycetes

1 reference

12 December 2020

MM 47755, a new benz[a]anthracene antibiotic from a streptomycete

1 reference

12 December 2020

Benzanthrins A and B, a new class of quinone antibiotics. I. Discovery, fermentation and antibacterial activity

1 reference

12 December 2020

Metabolic products of microorganisms. 234. Urdamycins, new angucycline antibiotics from Streptomyces fradiae. I. Isolation, characterization and biological properties

1 reference

12 December 2020

10.1021/ACS.JNATPROD.5B00601

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335269%20AND%20SRC:MED&resulttype=core&format=json